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10.1016/j.cmi.2021.02.001 http://scihub22266oqcxt.onion/10.1016/j.cmi.2021.02.001 33601009!7884234!33601009     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=33601009&cmd=llinks): Failed to open stream: HTTP request failed! 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Multicenter evaluation of the Panbio COVID-19 rapid antigen-detection test for the diagnosis of SARS-CoV-2 infection |pdf=|usr=}}{{33601009}} gab.com Text Multicenter evaluation of the Panbio COVID-19 rapid antigen-detection test for the diagnosis of SARS-CoV-2 infection JO: Clin Microbiol Infect http://www.kidney.de/pget.php?&tw=1&pmid=33601009 #FOAvip OBJECTIVES: The standard RT-PCR assay for coronavirus disease 2019 (COVID-19) is laborious and time-consuming, limiting testing availability. Rapid antigen-detection tests are faster and less expensive; however, the reliability of these tests must be validated before they can be used widely. The objective of this study was to determine the performance of the Panbio COVID-19 Ag Rapid Test Device (PanbioRT) (Abbott) in detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in nasopharyngeal swab specimens. METHODS: This prospective multicentre study was carried out in ten Spanish university hospitals and included individuals with clinical symptoms or epidemiological criteria of COVID-19. Only individuals with </=7 days from the onset of symptoms or from exposure to a confirmed case of COVID-19 were included. Two nasopharyngeal samples were taken to perform the PanbioRT as a point-of-care test and a diagnostic RT-PCR test. RESULTS: Among the 958 patients studied, 325 (90.5%) had true-positive results. The overall sensitivity and specificity for the PanbioRT were 90.5% (95%CI 87.5-93.6) and 98.8% (95%CI 98-99.7), respectively. Sensitivity in participants who had a threshold cycle (C(T)) < 25 for the RT-PCR test was 99.5% (95%CI 98.4-100), and in participants with </=5 days of the clinical course it was 91.8% (95%CI 88.8-94.8). Agreement between techniques was 95.7% (kappa score 0.90; 95%CI 0.88-0.93). CONCLUSIONS: The PanbioRT performs well clinically, with even more reliable results for patients with a shorter clinical course of the disease or a higher viral load. The results must be interpreted based on the local epidemiological context. Twit Text FOAVip Multicenter evaluation of the Panbio COVID-19 rapid antigen-detection test for the diagnosis of SARS-CoV-2 infection ????Clin Microbiol Infect http://www.kidney.de/pget.php?&tw=1&pmid=33601009 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33601009 #FOAvip English Wikipedia <ref>{{Cite pmid|33601009}}</ref> Multicenter evaluation of the Panbio COVID-19 rapid antigen-detection test for the diagnosis of SARS-CoV-2 infection #MMPMID33601009 Merino P; Guinea J; Munoz-Gallego I; Gonzalez-Donapetry P; Galan JC; Antona N; Cilla G; Hernaez-Crespo S; Diaz-de Tuesta JL; Gual-de Torrella A; Gonzalez-Romo F; Escribano P; Sanchez-Castellano MA; Sota-Busselo M; Delgado-Iribarren A; Garcia J; Canton R; Munoz P; Folgueira MD; Cuenca-Estrella M; Oteo-Iglesias J Clin Microbiol Infect 2021[Feb]; 27 (5): 758-61 PMID33601009show ga OBJECTIVES: The standard RT-PCR assay for coronavirus disease 2019 (COVID-19) is laborious and time-consuming, limiting testing availability. Rapid antigen-detection tests are faster and less expensive; however, the reliability of these tests must be validated before they can be used widely. The objective of this study was to determine the performance of the Panbio COVID-19 Ag Rapid Test Device (PanbioRT) (Abbott) in detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in nasopharyngeal swab specimens. METHODS: This prospective multicentre study was carried out in ten Spanish university hospitals and included individuals with clinical symptoms or epidemiological criteria of COVID-19. Only individuals with äMulticenter evaluation of the Panbio COVID-19 rapid antigen-detection (epmc).pdf DeepDyve Pubget Overpricing